NEO ERCP GUIDEWIRE

NEO ERCP GUIDEWIRE is an FDA 510(k)-cleared medical device (K123439) manufactured by Neometrics, Inc.. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 2, 2013. Regulation: 8.